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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382212Generated: November 1, 2026

Ciprofloxacin → HCID 13850789, compound

https://huagongshe.com/reaction/1382212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCiprofloxacinHCID 2764—
ReactantPotassium IodideHCID 4875—
ReactantTriethylamineHCID 8471—
ReactantChloromethyl trifluoromethyl sulfideHCID 3468030—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 13850789HCID 1385078933.7%

Reaction Steps

3.3 g (10 mmol) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are heated at 90° in 50 ml of dimethylformamide with 4 g (27 mmol) of trifluoromethylthiomethyl chloride, 2.1 g of triethylamine, 1.7 g of potassium iodide and 0.2 g of tetrabutylammonium iodide for 16 hours. The solution is poured into 50 ml of water and the precipitate is filtered off with suction and boiled up with methanol. 1.5 g of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-trifluoromethylthiomethyl-1-piperazinyl)-3-quinolinecarboxylic acid of melting point 247°-250° (with decomposition) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806539
Source datasetuspto-grants-1989_02
ORD IDord-dd39ef5f55064a55989d36b24fe33c2d
Source noteuspto-grants-1989_02